Journal
FULLERENES NANOTUBES AND CARBON NANOSTRUCTURES
Volume 31, Issue 9, Pages 815-827Publisher
TAYLOR & FRANCIS INC
DOI: 10.1080/1536383X.2023.2211695
Keywords
Graphite; phthalocyanines; ball-milling; composites; characterization
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Through dry ball-milling of graphite-phthalocyanine mixtures, low-cost and harmless graphite-phthalocyanine composites were successfully prepared. The composites exhibited high efficiency of phthalocyanine milling and improved exfoliation of graphite. However, their thermal stability was reduced compared to unprocessed graphite.
The hybrids of phthalocyanines with carbon nanotubes, graphene and graphene oxide were demonstrated previously to be promising for different catalytical, electrocatalytical and other applications. Nevertheless, the above carbon nanomaterials are toxic and relatively expensive. We attempted to substitute them by low-cost and harmless graphite, using dry ball-milling of graphite-phthalocyanine mixtures under mild conditions. According to scanning electron microscopy imaging and powder X-ray diffraction, the composites obtained exhibit the absence of crystalline phthalocyanine phase, which implies high efficiency of phthalocyanine milling. According to Raman spectroscopy data, the mechanochemical treatment does not provoke the formation of large amounts of defects in graphite, but instead helps its exfoliation. The composites were characterized by UV-visible spectroscopy and thermal gravimetric analysis, which showed that all of them exhibit a reduced thermal stability compared to unprocessed graphite by roughly 100-250 degrees C. The strength of interaction of phthalocyanines with a graphene sheet (as a graphite surface model), geometries and selected electronic parameters (frontier orbital and spin density distribution, HOMO-LUMO gap energies) of the resulting noncovalent complexes were analyzed at the PBE-D2/DNP theoretical level. The interactions of phthalocyanines with the graphene sheet are strong, with the calculated formation energies (absolute values) for the noncovalent complexes of 62.1-70.1 kcal/mol.
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